Responsibilities:
- Lead relevant data management efforts to coordinate study start-up activities, interim data cuts to support various activities
- Oversee database lock activities and ultimate archiving of study data
- May help in directing the overall data management standards and processes in a particular therapeutic area/program
- Review clinical study protocols and statistical analysis plans in the assigned therapeutic area (TA)
- Lead eCRF development and facilitate cross-functional reviews of eCRF content
- Oversee and direct database building activities, including review of edit check specifications and performance of user acceptance testing
- Monitor data collection, data cuts, coding, and cleaning by CROs through tracking of study metrics and targeted data reviews
- Review data management plans, CRF completion guidelines, external data transfer specifications and other study documentation in the assigned TA
- Represent data management in cross-functional meetings at the TA level
- May help in the SOP’s, checklists, templates development for data management by working with Director, Data Management
- May/Mayn’t oversee Data Managers on the assigned studies and may perform hands-on (overseeing) data management work
- May support the Director, Data Management on initiatives relevant to Imaging data, Biomarker data, Digital Health Technologies (DHT’s) data etc.,
- May support the Director, Data Management in evaluating DM relevant tools like reporting tools, data visualization tools, eConsent, etc.,
- Participates in other activities and meetings to support Data Management/Biometrics as necessary
Minimum Requirements:
- Excellent interpersonal skills and good conflict management and negotiation skills
- B.S. / B.A. in scientific discipline (minimum undergraduate degree required), with 7 years of Data Management experience and a minimum of 4 years of line management experience
- Experience with medical dictionaries, including MedDRA and WHODrug
- Proficient with electronic data capture (EDC) systems like Veeva EDC, Medidata-RAVE and the development of CRF/eCRF for clinical trials and its impact in database design/development
- Excellent organizational and time management skills with great attention to details
Top Skills
What We Do
BlueRock Therapeutics is a leading engineered cell therapy company with a mission to develop regenerative medicines for intractable diseases. BlueRock Therapeutics’ cell+gene platform harnesses the power of cells to create new medicines for neurology, cardiology, and immunology indications.
BlueRock Therapeutics’ cell differentiation technology recapitulates the cell’s developmental biology to produce authentic cell therapies, which are further engineered for additional function. Utilizing these cell therapies to replace damaged or degenerated tissue brings the potential to restore or regenerate lost function.
BlueRock’s culture is defined by scientific innovation, the highest ethical standards and an urgency to bring transformative treatments to all who would benefit. The company strives to be a top employer of scientific talent, empowering every member of the team to make meaningful and lasting contributions to the burgeoning field of regenerative medicine.
Become a BlueRocker! We are expanding our BlueRock team at all locations. Contact us via LinkedIn or our website to learn about rewarding career opportunities.







